Searchable abstracts of presentations at key conferences in endocrinology

ea0015p87 | Clinical practice/governance and case reports | SFEBES2008

Sarcoidosis associated hypercalcaemia and renal failure mimicking lymphoma

Bdiri Ashref , Smith Martin , Lawrence James

We describe two cases of sarcoidosis associated hypercalcaemia, renal failure and anaemia mimicking lymphoma. The diagnosis was made by lymph node biopsy. Within weeks of starting oral steroids, symptoms resolved and biochemical abnormalities almost normalized.Case 1: A 66-year-old lady, presented with generalized weakness, lymphadenopathy and splenomegaly. Hb 96 g/l, MCV 91, urea 16.6 mmol/l, creatinine 227 umol/l, eGFR 15 ml/min, serum calcium 3.4 mmol...

ea0013p88 | Clinical practice/governance and case reports | SFEBES2007

Hypoglycaemia secondary to leukamoid reaction

Elrishi MA , Bradley EJ , Lawrence IG

Introduction: Artifactual hypoglycaemia has been reported to occur in leukaemia, and also reported in polycythemia Vera, being caused by in vitro autoglycolysis due to an exaggerated consumption of glucose by white blood cells1. We report a case of recurrent hypoglycaemia found to be artifactual secondary to a leukamoid reaction.Case report: A 78-year-old lady with a poorly differentiated endometrial adenocarcinoma was referred to us with a hi...

ea0011p87 | Clinical case reports | ECE2006

Gitelman’s syndrome in pregnant, type 1 diabetic patient presented with foetal growth retardation, and bilateral hydronephrosis and hydroureter

Elrishi MA , Kilvert A , Sirnivasan B , Lawrence I

Gitelman’s syndrome (GS) is an autosomal recessive primary renal tubular disorder with hypokalemic metabolic alkalosis, hypocalciuria, and magnesium deficiency. The association of GS and type 1 diabetes is rare1, and bilateral hydronephrosis and hydroureter has not been reported.A 18-year-old female with known GS diagnosed at 17 years of age and type 1 diabetes diagnosed at 15 years of age was admitted to Leicester Royal Infirmary for pre...

ea0055oc4 | National Clinical Cases | SFEEU2018

Management of massive (up to 550 mm) bilateral adrenal masses in a non-adherent patient with 21-hydroxylase deficiency congenital adrenal hyperplasia:complex risk benefit analysis

Waterhouse Jasmin , Parvanta Laila , Akker Scott , Berney Dan , Lawrence Victor

Case history: We report a 38 year-old Caucasian woman with classical salt wasting congenital adrenal hyperplasia (CAH) who increasingly omitted medication in adolescence and eventually spent over 10 years without any adrenal replacement therapy or adrenal crises and became lost to follow up. When seen, she complained of increasing abdominal girth, fatigue, hirsutism, had type 2 diabetes, had never had a romantic/sexual relationship and was amenorrhoeic. Examination revealed ab...

ea0081ep14 | Adrenal and Cardiovascular Endocrinology | ECE2022

Adrenal sarcomas – Exceptionally rare or more common than thought? Prevalence in adrenalectomy specimens over 12 months period and presenting features.

Azman Nur , Lawrence James , Hayes Matthew , Douglas James , Bujanova Jana

Adrenal/periadrenal sarcomas are very rare entity of adrenal tumours. An epidemiological analysis of primary adrenal cancers found prevalence of adrenal sarcoma of 1.3% compared to adrenocortical carcinoma (ACC) 43.8%, neuroblastoma 39.7%, pheochromocytoma 10.9% and non-Hodgkin’s lymphoma 4.3% (1). In 2021, 26 adrenalectomies in adults were performed in our institution. 12/26 had malignant histology. 9/26 lesions were > 6 cm. 7/9 lesions > 6 cm were malignant (2 a...

ea0086p264 | Neuroendocrinology and Pituitary | SFEBES2022

Diabetes insipidus following a non-acute presentation of pituitary apoplexy – a rare presentation

Bastawrous Madona , Bhagi Ridhi , Roy Chowdhury Sharmistha , Cozma Lawrence

Introduction: Pituitary apoplexy (PA) is a rare endocrine emergency with less described entity being its subacute/non-acute presentation. Incidence of PA is difficult to determine, varying 2%-12% of pituitary adenoma. Hypopituitarism in PA is observed in up to 70% of cases with diabetes Insipidus (DI) observed in <5% of cases and mostly transient.Case description: 82-year old female with pituitary macroprolactinoma (1.5 cm) presented with 3-week hist...

ea0059p045 | Bone and calcium | SFEBES2018

Evaluation of effect of primary hyperparathyroidism and parathyroidectomy on blood pressure

Boregowda Kusuma , Roychowdhury Sharmistha , Cozma Lawrence , Shering Stephen

Primary hyperparathyroidism (PHPT) is one of the common endocrine conditions and is frequently associated with hypertension and increased cardiovascular mortality but this association is not well recognised. The purpose of this study was to evaluate the effect of parathyroidectomy on blood pressure. The data of 112 patients who attended our out patients clinic over the period of 12 months, with the confirmed diagnosis of primary hyperparathyroidism was evaluated. Average age w...

ea0070ep529 | Thyroid | ECE2020

Recurrent subacute thyroiditis associated with microscopic polyangiitis (ANCA positive vasculitis)

Lawrence Townsend Adam , Talapatra Indrajit , James Tymms David , Kumar Mohit

A 56 year old lady was investigated by her GP for arthralgia and found to be thyrotoxic (TSH < 0.01 mU/l, free T4 34.8 (10–20 pmol/l), TPO 50 (<35 IU/ml)). She gave a history of anterior uveitis some 20 years earlier. She was commenced on carbimazole and referred to the endocrinology clinic, where her thyroid function rapidly normalised and a biochemical diagnosis of subacute thyroiditis was made. Thyroid pertechnatate scan showed reduced uptake throughout the gl...

ea0028p71 | Clinical practice/governance and case reports | SFEBES2012

Long-term remission of postmenopausal ovarian hyperandrogenism may occur following a period of gonadotropin-releasing hormone (GnRH) agonist therapy

Lawrence Carly , Dyke Claire , Cox Sue , Smith Jamie

Excessive ovarian androgen production developing in post-menopausal women can be associated with severe hirsutism and virilisation. In the absence of an identifiable androgen-secreting tumour, medical therapy rather than surgical removal is a potential treatment option. Despite this, the role and outcomes of medical therapy are not well characterised in this context. We present the long-term outcomes of 2 women with postmenopausal ovarian hyperandrogenism, both of whom were tr...

ea0015p2 | Bone | SFEBES2008

Hypocalcaemia in pregnancy: vitamin D deficiency and pseudohypoparathryoidism type 1b

Lawrence Christopher , Mapplebeck Sarah , Harnett Patrick , Almond Mike

FH, a 36-year-old female of Afghan origin, resident in the UK for 4 years, was referred to the medical services by her obstetrician 9 days postpartum with symptomatic hypocalcaemia. Biochemical investigations confirmed a low corrected calcium (1.43 mmol/l, 2.1–2.6 mmol/l), elevated phosphate (1.76, 0.8–1.45 mmol/l) and alkaline phosphatase (156, 30–130 U/l). Twenty-five hydroxy vitamin D was 16 nmol/l (15–100) with elevated PTH (21.76 pmol/l, 1.05–6.83...